Quantized Energy (Planck)

Modified From-http://www2.asd.k12.ak.us/hauser/curriculum/html/Chemistry/Unit%209%20Modern%20Atomic%20Theory/Handouts%20and%20Notes/Unit_09_Light_(Handout).htm

Quantized energy

In 1900, a German scientist named Max Planck wrote an equation to show this the relationship between energy and frequency of electromagnetic radiation : 

E = hn 

where E is the energy of a bit of light called a quantum, A quantum is the smallest bit of electromagnetic radiation that can be emitted.  It is also called a photon of light or small “packet” of electromagnetic radiation.    The “h” in the above equation is a very small constant called “Planck’s constant” (6.626068 × 10-34 J s) and “n” is the frequency of the radiation.  Through various experiments of Planck and Albert Einstein, it came to be accepted that light has properties of particles as well as waves.  Planck’s “quantum” idea became the basis for the modern understanding of atomic structure.  In the above equation, as the frequency of radiation increases, its energy increases by the increment “h”.  In other words, energy was not continuous, it was quantized – only certain energies are allowed.  Continuous energy and quantized energy can be likened to a  ramp versus a set of stairs connecting two levels of a building.   The ramp is analogous to continuous energy – you can sit at any position along the ramp and thus be at any elevation between the two levels.  The stairs are analogous to quantized or discrete energy – you can only sit at certain elevations between the two levels and nowhere in between.  You may sit only on the steps, not in between the steps.  Only certain elevations are allowed. 

Spectra of elements

So what does all this stuff about waves and light and Plancks have to do with chemistry?  It had been known for many years that when samples of elements were heated up or energized with electricity, they burned or glowed a certain color, not the entire rainbow of colors like we see from white light. (Below)

Image:Spectral lines continous.png

 Each element seemed to have its own characteristic color.  If we energize a sample of hydrogen with electricity, we see a light purple color and if we energize a sample of neon with electricity we see the characteristic bright orange color that is so common in “neon signs”.  If we pass this light through a prism, which separates the colors of light like rain separates the colors of white light into a rainbow, we see not a rainbow of continuous colors but only certain, sharp lines of color.  We see discreet energy levels, not continuous energy levels.  Only certain colors are seen, not the whole rainbow.  Why is this so?  Between 1911 and 1913, the Danish scientist, Niels Bohr, tried to explain the line spectrum of the element hydrogen which contains 5 and only 5 distinct lines of color, each with their own energy, wavelength and frequency.  Only 3 or 4 of the lines are bright enough to see, below.   Starting at the left, violet at 410nm, blue at 434nm, green at 486nm and red at 656nm. 

 

Bohr imagined  hydrogen’s lone electron as orbiting around the nucleus just like planets orbit around the sun, but at a fixed distance from the nucleus.

 

The energy of the electron is lowest when it is quite close to the nucleus and this state of the electron is called the ground state of the atom.    When an atom gains extra energy ( through heating or electricity), the electron moves farther away from the atom.  There is a natural attraction of the negatively charged electron for the positively charged nucleus so it follows that it would take energy to move the electron away from this desirable situation.  Picture one end of a rubber band pulled snug around a finger.  The finger is the nucleus and the other end of the rubber band is the electron.  By stretching  the rubber band, energy is added and one end of the band (the electron) is moved farther away from the finger (the nucleus).  This is called an excited state of the atom.  If one now lets go of the rubber band, it comes slamming back into the finger and the excess energy added a moment ago is released as heat on the finger.  The energy released depends on how much added energy was used to stretch the rubber band in the first place.  Bohr guessed that electrons in atoms had only certain allowed orbits, only certain distances from the nucleus.  The electron could therefore absorb only certain energies to take them to these fixed distances and when this excess energy was released, only certain or quantized energies were released as light.  This would explain why only certain colors (and therefore certain wavelengths of light) were observed when a hydrogen atom was excited.  The farther an electron dropped back towards the nucleus, the more energy it would release and the shorter the wavelength of light that would be observed.  The violet line of the hydrogen spectrum was light of greater energy than the red line in the spectrum because the electron had fallen much farther than it did in another hydrogen atom that released the red light.  All 5 lines are seen since billions of atoms are being excited to various but very limited degrees.  So, had Bohr figured it out?  Could he predict the line spectra of other elements based on this idea of electrons jumping up and down between only certain allowed orbits?  He could not.  He tried his theory with other atoms and it did not work.  From this analysis, it was determined that electrons do not  move around the nucleus in circular orbits.  In fact, it is still not known just how the electrons move around the nucleus. 

Flash from-http://spiff.rit.edu/classes/phys301/lectures/spec_lines/Atoms_Nav.swf

 

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